Key result
A 37-year-old male with a rare mural thrombus in a normal descending thoracic aorta was successfully managed conservatively with anticoagulation therapy.
Why the study?
Thrombus formation in a normal appearing descending thoracic aorta is rarely reported, and its true incidence, prevalence, and exact etiopathogenesis remain uncertain.
Case Report (n=1)
No
Aortic mural thrombus in a normal appearing descending thoracic aorta is a rare entity that can be successfully managed with therapeutic anticoagulation in select patients.
Answers are grounded in this paper and cite their sources.
Supports anticoagulation in select aortic mural thrombus cases; leaves open need for prospective data.
Occurrence of a mural thrombus in a diseased descending thoracic aorta (atherosclerotic or aneurysmal) is a well-known and commonly encountered vascular entity. However, thrombus formation in a normal appearing descending thoracic aorta (NADTA) is rarely reported in literature so far. We present an unusual case report with a brief literature review of an aortic mural thrombus (AMT) in descending thoracic aorta in a young male. He presented at our center in the emergency department with acute onset abdominal pain and underwent a contrast enhanced CT scan that confirmed mural thrombus in NADTA. He was conservatively managed with anticoagulation therapy. He had a family history of venous thromboembolism (VTE) in his brother, who had experienced two episodes of deep vein thrombosis at the age of 40 years, managed with anticoagulation. The true incidence, prevalence and exact etiopathogenesis of AMT is still uncertain. However, certain predisposing factors have been described in literature. Through this case report, we aim to highlight the significance of increased awareness required among the general surgeons and radiologists for early and correct diagnosis of this condition, to prevent the unforeseen complications of distal organ/acute limb ischaemia and its associated morbidity and mortality.
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Jayesh Sagar (2020) conducted a case report in Mural thrombus in normal descending thoracic aorta (n=1). Anticoagulation therapy (Tinzaparin and oral warfarin) was evaluated. A 37-year-old male with a rare mural thrombus in a normal descending thoracic aorta was successfully managed conservatively with anticoagulation therapy.
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